首页> 美国卫生研究院文献>Oncology Letters >Effects of anti-CD44 monoclonal antibody IM7 carried with chitosan polylactic acid-coated nano-particles on the treatment of ovarian cancer
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Effects of anti-CD44 monoclonal antibody IM7 carried with chitosan polylactic acid-coated nano-particles on the treatment of ovarian cancer

机译:壳聚糖聚乳酸包裹的纳米颗粒携带的抗CD44单克隆抗体IM7对卵巢癌的治疗作用

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摘要

Failure in early diagnosis and ineffective treatment are the major causes of ovarian cancer mortality. Hyaluronan and its receptor, cluster of differentiation (CD)44, have been considered to be valid targets for treating cancer. The anti-CD44 monoclonal antibody IM7 is effective in treating ovarian cancer; however, its toxicity should not be ignored. The present study has developed a new drug carrier system composed of chitosan nano-particles coated with polylactic acid (PLA) to improve the treatment efficacy and reduce toxicity. An ionic crosslinking method and 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride/N-hydroxysuccinimide were used to prepare the IM7 antibody, which was loaded with chitosan nano-particles. The surfaces of the nano-particles were coated with PLA to generate PLA-chitosan-IM7. Subsequently, transmission electron microscopy (TEM) was used to observe the size and zeta potential of the nano-particles. In addition, a spectrophotometer was used to calculate the loading rate and release rate of the nano-particles in acidic and neutral environments. MTT assay was used to evaluate the anti-proliferative effect of PLA-chitosan-IM7 on the human ovarian cancer cell line HO-8910PM. In addition, an in vivo imaging system was used to further investigate the effect of PLA-chitosan-IM7 on the treatment of mice with ovarian cancer. A total of 35 days subsequent to PLA-chitosan-IM7 treatment, all animals were sacrificed by CO2, and the tumors were removed and weighted. The PLA-chitosan-IM7 nano-particles were successfully prepared, since TEM revealed that their size was 300–400 nm and their zeta potential was +25 mV. According to the spectrophotometry results, the loading rate was 52%, and PLA-chitosan-IM7 exhibited good resistance to acids. MTT assay demonstrated that PLA-chitosan-IM7 could suppress the proliferation of HO-8910PM cells in vitro. The in vivo imaging system revealed that PLA-chitosan-IM7 was effective in controlling the development of human ovarian cancer cells and the tumor weight. These results suggest that PLA-chitosan-IM7 could be effective in treating cancers in vitro and in vivo, which may provide a novel approach to enhance the effectiveness of anti-CD44 treatment while reducing its toxicity.
机译:早期诊断失败和治疗无效是卵巢癌死亡的主要原因。透明质酸及其受体,分化簇(CD)44被认为是治疗癌症的有效靶标。抗CD44单克隆抗体IM7对卵巢癌有效。但是,其毒性不容忽视。本研究开发了一种新的药物载体系统,该系统由包覆有聚乳酸(PLA)的壳聚糖纳米颗粒组成,可提高治疗效果并降低毒性。离子交联法和1-乙基-3-(3-二甲基氨基丙基)碳二亚胺盐酸盐/ N-羟基琥珀酰亚胺用于制备IM7抗体,该抗体负载有壳聚糖纳米颗粒。纳米粒子的表面涂覆有PLA生成PLA-壳聚糖-IM7。随后,使用透射电子显微镜(TEM)观察纳米颗粒的尺寸和ζ电势。另外,使用分光光度计来计算在酸性和中性环境中纳米颗粒的负载率和释放率。 MTT法用于评估PLA-壳聚糖-IM7对人卵巢癌细胞系HO-8910PM的抗增殖作用。另外,使用体内成像系统进一步研究PLA-壳聚糖-IM7对卵巢癌小鼠的治疗作用。 PLA-壳聚糖-IM7处理后总共35天,所有动物均被CO2处死,并切除肿瘤并称重。成功制备了PLA-壳聚糖-IM7纳米颗粒,因为TEM显示其尺寸为300-400 nm,ζ电位为+25 mV。根据分光光度法的结果,负载率为52%,并且PLA-壳聚糖-IM7表现出良好的耐酸性。 MTT分析表明,PLA-壳聚糖-IM7可以抑制HO-8910PM细胞的体外增殖。体内成像系统显示,PLA-壳聚糖-IM7在控制人卵巢癌细胞的发育和肿瘤重量方面有效。这些结果表明,PLA-壳聚糖-IM7可能在体内和体外治疗癌症方面有效,这可能提供一种新颖的方法来增强抗CD44治疗的有效性,同时降低其毒性。

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